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Cytotoxic Efficacy of Photodynamic Therapy in Osteosarcoma Cells In Vitro
Published on: March 18, 2014
Soft X-ray-Enhanced Reactive Oxygen Species Generation in Mesoporous Titanium Peroxide and the Application in Tumor
Zideng Dai1,2, Junkai Cao1,2, Zhaoming Guo3
1State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, China.
Abstract:
Mesoporous titanium peroxide TiO nanospheres with a high surface area are synthesized for the application of an advanced drug system. The mesoporous TiO nanospheres have a high specific surface area of 681.89 m2/g and suitable pore size (∼3 nm) that can effectively upload doxorubicin (DOX) and possesses a high drug storage capacity of 146.08%. They show a distinct ability to produce reactive oxygen species (ROS) in response to X-ray irradiation, which can effectively improve the radiotherapy in tumor treatment using the lung cancer cell line. The ROS generation of TiO is more than ten-fold higher than that of TiO2. No apparent toxicity is found for the TiO material itself without X-ray irradiation. In vitro and in vivo experiments show that TiO/DOX nanodrugs significantly enhance cytotoxicity in response to X-ray irradiation. CCK8 assays display that the TiO/DOX nanodrug has higher cancer treatment efficiency in response to X-ray irradiation because of the synergistic effect of chemotherapy and generation of ROS. In the in vivo experiments using lung cancer tumor-bearing mice model, the tumor inhibition rate in the TiO/DOX + X-ray group increased by 90.4% compared to the untreated control group, showing a good synergistic chemo-radiotherapy effect in tumor treatment.

